Canonical Allele Identifier: PA645416776
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 339886
ClinVar RCV Id: RCV000263703 RCV002523178
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_652763.1:p.Ala196Val
CA10019225
NM_144492.3:c.587C>T