Canonical Allele Identifier: PA2826440229
Gene: CDH13 HGNC NCBI

Linked Data

ClinVar Variation Id: 722627
ClinVar RCV Id: RCV000896293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001248.1:p.Ser709Thr
CA8196980
NM_001257.4:c.2126G>C