Canonical Allele Identifier: PA338487
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Leu21Phe
CA338485
NM_004360.5:c.61C>T