Canonical Allele Identifier: PA102173
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 56008
ClinVar RCV Id: RCV000049417
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.His220Pro
CA144113
NM_000111.3:c.659A>C