Canonical Allele Identifier: PA2580104056
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2164286
ClinVar RCV Id: RCV003073566 RCV004073104
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Tyr232Cys
CA361705541
NM_000112.4:c.695A>G