Canonical Allele Identifier: PA2825411551
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2574892
ClinVar RCV Id: RCV003319789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Trp6Arg
CA414606348
NM_001042537.2:c.16T>A
CA414606349
NM_001042537.2:c.16T>C