Canonical Allele Identifier: PA2825692498
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 462156
ClinVar RCV Id: RCV000526328 RCV001260727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Pro173Leu
CA378921066
NM_001130442.3:c.518C>T