Canonical Allele Identifier: PA2828165227
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 5331
ClinVar RCV Id: RCV000005657 RCV000790223 RCV002512812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352017.1:p.Arg207Cys
CA253467
NM_001365088.1:c.619C>T