Canonical Allele Identifier: PA2826295595
Gene: CDH13 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001207418.1:p.Ser670Thr
CA8196980
NM_001220489.2:c.2009G>C