Canonical Allele Identifier: PA216261
Gene: CLDN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 64491
ClinVar RCV Id: RCV000054678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153572.1:p.Asn119Lys
CA216260
NM_001160100.2:c.357C>A
CA388484206
NM_001160100.2:c.357C>G