Canonical Allele Identifier: PA295172
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 159933
ClinVar RCV Id: RCV000147542 RCV000224732 RCV000462225 RCV002312660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Ala9Ser
CA295170
NM_006359.3:c.25G>T