Canonical Allele Identifier: PA891858699
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 568090
ClinVar RCV Id: RCV000688334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065759.1:p.Ser978Asn
CA409207603
NM_020708.5:c.2933G>A