Canonical Allele Identifier: PA2826127085
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_001171122.1:p.Ala163Thr
CA318518
NM_001177651.2:c.487G>A