Canonical Allele Identifier: PA2579930637
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1509551
ClinVar RCV Id: RCV002017989 RCV003332372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ile46Val
CA378924771
NM_001130442.3:c.136A>G