Canonical Allele Identifier: PA195507
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186668
ClinVar RCV Id: RCV000166300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Ser793Arg
CA195505
NM_004360.5:c.2379T>G
CA396471112
NM_004360.5:c.2377A>C
CA396471126
NM_004360.5:c.2379T>A