Canonical Allele Identifier: PA2829948476
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003386
ClinVar RCV Id: RCV001299932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065759.1:p.Pro1001Ser
CA409207812
NM_020708.5:c.3001C>T