Canonical Allele Identifier: PA2825617700
Gene: MET HGNC NCBI
ClinVar RCV:
RCV003597005
ClinVar Variation:
2753653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Glu28Val
CA368968306
NM_001127500.3:c.83A>T