Canonical Allele Identifier: PA2825852781
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2711156
ClinVar RCV Id: RCV003513083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Leu317Val
CA415086749
NM_001142806.1:c.949C>G