Canonical Allele Identifier: PA1139677146
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 887611
ClinVar RCV Id: RCV001120453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Phe742Cys
CA395994719
NM_001126108.2:c.2225T>G