Canonical Allele Identifier: PA110443
Gene: SLC26A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 50910
ClinVar RCV Id: RCV000043625 RCV002247429 RCV002513638
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180405.1:p.Glu812Lys
CA143849
NM_001193476.2:c.2434G>A