Canonical Allele Identifier: PA916068422
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_602298.2:p.Val228Leu
CA216183
NM_134426.3:c.682G>C