Canonical Allele Identifier: PA658661522
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 453151
ClinVar RCV Id: RCV000520357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Ala21Pro
CA414606436
NM_006359.3:c.61G>C