Canonical Allele Identifier: PA658826994
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 550239
ClinVar RCV Id: RCV000664934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asn712del
CA658821811
NM_000441.2:c.2135_2137del