Canonical Allele Identifier: PA2580198913
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2128760
ClinVar RCV Id: RCV003057735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Leu80Phe
CA378921178
NM_001318054.2:c.240G>T
CA378921179
NM_001318054.2:c.240G>C