Canonical Allele Identifier: PA2741859586
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2820359
ClinVar RCV Id: RCV003627985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Asn93Lys
CA378921078
NM_001318054.2:c.279C>A
CA378921080
NM_001318054.2:c.279C>G