Canonical Allele Identifier: PA1139687958
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 946716
ClinVar RCV Id: RCV001217639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Gly1051Asp
CA9887777
NM_001134771.2:c.3152G>A