Canonical Allele Identifier: PA2825851962
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 572616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Pro31Leu
CA415076214
NM_001142805.2:c.92C>T