Canonical Allele Identifier: PA2580104161
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2187310
ClinVar RCV Id: RCV002623492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Lys615del
CA3505503
NM_000112.4:c.1843_1845del