Canonical Allele Identifier: PA2825075665
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3163841
ClinVar RCV Id: RCV004456658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Trp613Leu
CA361709006
NM_000112.4:c.1838G>T