Canonical Allele Identifier: PA2579931243
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 618166
ClinVar RCV Id: RCV000756250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Met72Leu
CA378924601
NM_001130442.3:c.214A>T
CA378924603
NM_001130442.3:c.214A>C