Canonical Allele Identifier: PA238859
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 193338
ClinVar RCV Id: RCV000173403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Met25Leu
CA238858
NM_001042537.2:c.73A>C
CA414606459
NM_001042537.2:c.73A>T