Canonical Allele Identifier: PA2829600873
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2416915
ClinVar RCV Id: RCV003109166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Thr74Ala
CA378924589
NM_005343.4:c.220A>G