Canonical Allele Identifier: PA2829583126
Gene: SLC12A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1996507
ClinVar RCV Id: RCV002823757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005126.1:p.Val151Gly
CA391612830
NM_005135.2:c.452T>G