Canonical Allele Identifier: PA2573308908
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1437577
ClinVar RCV Id: RCV001948765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ser39Thr
CA378924818
NM_176795.5:c.115T>A