Canonical Allele Identifier: PA2579931418
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375961
ClinVar RCV Id: RCV000421560 RCV000431895 RCV002230756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly12Arg
CA16602439
NM_001130442.3:c.34G>C