Canonical Allele Identifier: PA915974082
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 657261
ClinVar RCV Id: RCV000813836 RCV003413636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Arg3Trp
CA414606333
NM_006359.3:c.7C>T