Canonical Allele Identifier: PA658803108
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 505477
ClinVar RCV Id: RCV000607476 RCV003558453
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Met21Val
CA4432355
NM_000441.2:c.61A>G