Canonical Allele Identifier: PA103633
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12604
ClinVar RCV Id: RCV000013438 RCV000157913 RCV000439514 RCV000781469 RCV001376018 RCV001813187 RCV002476960 RCV003390677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly13Asp
CA256488
NM_001130442.3:c.38G>A