Canonical Allele Identifier: PA1139693135
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 981949
ClinVar RCV Id: RCV001265206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile363Leu
CA368838700
NM_000441.2:c.1087A>C