Canonical Allele Identifier: PA122552
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12608
ClinVar RCV Id: RCV000013442 RCV000485616 RCV002272015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Glu63Lys
CA122551
NM_005343.4:c.187G>A