Canonical Allele Identifier: PA915976692
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 643672
ClinVar RCV Id: RCV000797434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Asn977Lys
CA315644443
NM_001134771.2:c.2931C>A
CA409207433
NM_001134771.2:c.2931C>G