Canonical Allele Identifier: PA2825102956
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 524880
ClinVar RCV Id: RCV000628759 RCV001013433 RCV001756034 RCV002483765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Thr621Ile
CA4448286
NM_000245.4:c.1862C>T