Canonical Allele Identifier: PA207288
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 212218
ClinVar RCV Id: RCV000193658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036002.1:p.Ile107Met
CA207287
NM_001042537.2:c.321T>G