Canonical Allele Identifier: PA2825411550
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 450956
ClinVar RCV Id: RCV000523044 RCV002528239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Trp6Cys
CA336084217
NM_001042537.2:c.18G>C
CA414606354
NM_001042537.2:c.18G>T