Canonical Allele Identifier: PA658668577
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 446451
ClinVar RCV Id: RCV000515721
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Pro76Ser
CA368845431
NM_000441.2:c.226C>T