Canonical Allele Identifier: PA2827340518
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_001317581.1:p.Ala131Thr
CA318518
NM_001330652.2:c.391G>A