Canonical Allele Identifier: PA2580278785
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2000338
ClinVar RCV Id: RCV002797365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Lys147Asn
CA341739050
NM_002524.5:c.441G>T
CA341739051
NM_002524.5:c.441G>C