Canonical Allele Identifier: PA645420029
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 429629
ClinVar RCV Id: RCV000494024 RCV001507028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Gly46Asp
CA10524597
NM_006359.3:c.137G>A