Canonical Allele Identifier: PA2828808539
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305512
ClinVar RCV Id: RCV001768719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366039.1:p.Ile26Val
CA414606806
NM_001379110.1:c.76A>G