Canonical Allele Identifier: PA2826295636
Gene: CDH13 HGNC NCBI
ClinVar RCV:
RCV000896293
ClinVar Variation:
722627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001207419.1:p.Ser455Thr
CA8196980
NM_001220490.2:c.1364G>C