Canonical Allele Identifier: PA915996847
Gene: CLDN19 HGNC NCBI

Linked Data

ClinVar Variation Id: 297340
ClinVar RCV Id: RCV000295255 RCV001516776
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001172046.1:p.Gly172Ser
CA801335
NM_001185117.2:c.514G>A