Canonical Allele Identifier: PA2579931861
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1987678
ClinVar RCV Id: RCV002790114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg41Pro
CA378924801
NM_001130442.3:c.122G>C