Canonical Allele Identifier: PA102285
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4091
ClinVar RCV Id: RCV000004309 RCV000675095 RCV000797878 RCV003472968
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Ala715Val
CA252994
NM_000112.4:c.2144C>T