Canonical Allele Identifier: PA2825103616
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2567671
ClinVar RCV Id: RCV003311360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Ser966Arg
CA368986937
NM_000245.4:c.2896A>C
CA368986949
NM_000245.4:c.2898T>A
CA368986950
NM_000245.4:c.2898T>G