Canonical Allele Identifier: PA2825924986
Gene: CLDN14 HGNC NCBI

Linked Data

ClinVar Variation Id: 228520
ClinVar RCV Id: RCV000215729 RCV002291596
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139551.1:p.Asp187Tyr
CA10019232
NM_001146079.2:c.559G>T