Canonical Allele Identifier: PA916014442
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 819155
ClinVar RCV Id: RCV001011454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Thr472Ser
CA396462949
NM_004360.5:c.1414A>T
CA396462955
NM_004360.5:c.1415C>G