Canonical Allele Identifier: PA915977768
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 522471
ClinVar RCV Id: RCV000625612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119580.2:p.Ser91Pro
CA395977818
NM_001126108.2:c.271T>C