Canonical Allele Identifier: PA2579931248
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1711130
ClinVar RCV Id: RCV002292424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Met67Leu
CA378924639
NM_001130442.3:c.199A>T
CA378924640
NM_001130442.3:c.199A>C