Canonical Allele Identifier: PA915988453
Gene: CLDN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 64491
ClinVar RCV Id: RCV000054678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008915.1:p.Asn140Lys
CA216260
NM_006984.5:c.420C>A
CA388484206
NM_006984.5:c.420C>G