Canonical Allele Identifier: PA2830512577
Gene: SLC26A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356871
ClinVar RCV Id: RCV001880535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996767.1:p.Pro54Ala
CA368737103
NM_206884.3:c.160C>G