Canonical Allele Identifier: PA2825142854
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 522471
ClinVar RCV Id: RCV000625612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Ser91Pro
CA395977818
NM_000339.3:c.271T>C