Canonical Allele Identifier: PA645375962
Gene: SLC9A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 426935
ClinVar RCV Id: RCV000489661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775924.1:p.Ile581Thr
CA354871319
NM_173653.4:c.1742T>C