Canonical Allele Identifier: PA318519
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207239
ClinVar RCV Id: RCV000189407 RCV001051665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Ala183Thr
CA318518
NM_006359.3:c.547G>A