Canonical Allele Identifier: PA180651
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 177717
ClinVar RCV Id: RCV000154323 RCV000671675 RCV000945063 RCV001375309 RCV001785479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Glu737Asp
CA180650
NM_000441.2:c.2211G>C
CA368846081
NM_000441.2:c.2211G>T