Canonical Allele Identifier: PA2579931358
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1362265
ClinVar RCV Id: RCV001900092
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly75Arg
CA5779384
NM_001130442.3:c.223G>A
CA378924583
NM_001130442.3:c.223G>C