Canonical Allele Identifier: PA2829600783
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1523510
ClinVar RCV Id: RCV002038934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Glu49Gln
CA378924751
NM_005343.4:c.145G>C