Canonical Allele Identifier: PA645428240
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 358535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Asn753Ser
CA4433530
NM_000111.3:c.2258A>G