Canonical Allele Identifier: PA915977759
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 319888
ClinVar RCV Id: RCV000328265 RCV000963131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Ser27Arg
CA8068907
NM_001126108.2:c.81C>G
CA395976251
NM_001126108.2:c.79A>C
CA395976255
NM_001126108.2:c.81C>A