Canonical Allele Identifier: PA160426
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 134646
ClinVar RCV Id: RCV000121342 RCV000567367 RCV001391320 RCV001548349 RCV003492526 RCV001292685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Met35Leu
CA160424
NM_001127500.3:c.103A>T
CA368968345
NM_001127500.3:c.103A>C