Canonical Allele Identifier: PA2825592323
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 297346
ClinVar RCV Id: RCV000302592 RCV001052078
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116867.1:p.Ile22Thr
CA801482
NM_001123395.2:c.65T>C