Canonical Allele Identifier: PA2825101652
Gene: MET HGNC NCBI
ClinVar RCV:
RCV003764428
ClinVar Variation:
2919100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Val6Gly
CA164887563
NM_000245.4:c.17T>G