Allele Registry

Canonical Allele Identifier: PA658668577

Gene: SLC26A4 HGNC NCBI

ClinVar Allele:

439900

ClinVar RCV:

RCV000515721

ClinVar Variation:

446451

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