Canonical Allele Identifier: PA2741861627
Gene: MET HGNC NCBI
ClinVar RCV:
RCV003764428
ClinVar Variation:
2919100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Val6Gly
CA164887563
NM_001324401.3:c.17T>G