Canonical Allele Identifier: PA103639
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12606
ClinVar RCV Id: RCV000013440 RCV000149831 RCV000207504 RCV000424247 RCV000425964 RCV000417661 RCV000433893 RCV000444110 RCV000445225 RCV000423190 RCV000426653 RCV000439052 RCV000439954 RCV000420958 RCV000445336 RCV000428812 RCV000431688 RCV000434069 RCV000436007 RCV000436205 RCV000441514 RCV000678903 RCV000762847 RCV001813188 RCV003421918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly13Cys
CA295247
NM_001130442.3:c.37G>T