Canonical Allele Identifier: PA2499271534
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008693
ClinVar RCV Id: RCV001306071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Glu17Asp
CA415076029
NM_005629.4:c.51G>T
CA415076030
NM_005629.4:c.51G>C