Canonical Allele Identifier: PA348614
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 220015
ClinVar RCV Id: RCV000204369 RCV001027373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Pro277Ser
CA348612
NM_004360.5:c.829C>T