Canonical Allele Identifier: PA180889
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40437
ClinVar RCV Id: RCV000154506 RCV000519779 RCV000680288 RCV001085194 RCV001261051 RCV001813234 RCV002257370 RCV003944864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Asn86Thr
CA180888
NM_005343.4:c.257A>C