Canonical Allele Identifier: PA2829948502
Gene: SLC12A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058068
ClinVar RCV Id: RCV001367159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065759.1:p.Pro1037Leu
CA409208356
NM_020708.5:c.3110C>T