Canonical Allele Identifier: PA645387196
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 227949
ClinVar RCV Id: RCV000221470 RCV000726317 RCV001004619 RCV001004774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser49Arg
CA4432373
NM_000441.2:c.147C>G
CA368845226
NM_000441.2:c.145A>C
CA368845237
NM_000441.2:c.147C>A