Canonical Allele Identifier: PA109463
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 691508
ClinVar RCV Id: RCV001004625 RCV001389158 RCV003235420
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Met147Val
CA4432481
NM_000441.2:c.439A>G