Allele Registry

Canonical Allele Identifier: PA2499301288

Gene: HRAS HGNC NCBI

ClinVar Allele:

994569

ClinVar RCV:

RCV001307584

ClinVar Variation:

1010014

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Phe90Ser	CA378924377 NM_176795.5:c.269T>C