Canonical Allele Identifier: PA916003206
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 658337
ClinVar RCV Id: RCV000815145
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Val49Leu
CA415076485
NM_005629.4:c.145G>C
CA415076487
NM_005629.4:c.145G>T