Allele Registry

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Canonical Allele Identifier: PA2825411608

Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798016

ClinVar RCV Id: RCV002441830 RCV003102909

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001036002.1:p.Phe98Leu	CA414606935 NM_001042537.2:c.292T>C CA414606939 NM_001042537.2:c.294C>A CA414606940 NM_001042537.2:c.294C>G