Canonical Allele Identifier: PA2829948497
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052598
ClinVar RCV Id: RCV001360816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065759.1:p.Asp1031His
CA409208220
NM_020708.5:c.3091G>C