Canonical Allele Identifier: PA2825851942
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008693
ClinVar RCV Id: RCV001306071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Glu17Asp
CA415076029
NM_001142805.2:c.51G>T
CA415076030
NM_001142805.2:c.51G>C