Canonical Allele Identifier: PA2825101700
Gene: MET HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Glu28Val
CA368968306
NM_000245.4:c.83A>T