Canonical Allele Identifier: PA2579930617
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2850846
ClinVar RCV Id: RCV003628532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ala66Val
CA378924641
NM_001130442.3:c.197C>T