Canonical Allele Identifier: PA2580157136
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2101967
ClinVar RCV Id: RCV003026272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Phe1055Leu
CA409208241
NM_001134771.2:c.3163T>C
CA409208253
NM_001134771.2:c.3165C>A
CA409208256
NM_001134771.2:c.3165C>G