Allele Registry

Canonical Allele Identifier: PA116648

Gene: SLC26A2 HGNC NCBI

ClinVar RCV:

RCV000004311

RCV000055758

ClinVar Variation:

4096

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Gln454Pro	CA116646 NM_000112.4:c.1361A>C