Canonical Allele Identifier: PA645492696
Gene: CLDN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 288149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066924.1:p.Ala14Val
CA2753644
NM_021101.5:c.41C>T