Canonical Allele Identifier: PA1139687950
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 852888
ClinVar RCV Id: RCV001057598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Pro1044Leu
CA409208064
NM_001134771.2:c.3131C>T