Allele Registry

Canonical Allele Identifier: PA2579933406

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV002801443

ClinVar Variation:

1993499

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Asn85Asp	CA5779379 NM_001130442.3:c.253A>G