Canonical Allele Identifier: PA216184
Gene: SLC26A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 64457
ClinVar RCV Id: RCV000054644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035544.1:p.Val207Leu
CA216183
NM_001040454.1:c.619G>C