Canonical Allele Identifier: PA2825409981
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2775944
ClinVar RCV Id: RCV003662849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035962.1:p.Val209Ile
CA391611709
NM_001042497.2:c.625G>A