Canonical Allele Identifier: PA2825411571
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062813
ClinVar RCV Id: RCV001372571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Ala33Ser
CA10524591
NM_001042537.2:c.97G>T