Canonical Allele Identifier: PA916073594
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 228520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_652763.1:p.Asp187Tyr
CA10019232
NM_144492.3:c.559G>T