Canonical Allele Identifier: PA891852060
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 572616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Pro31Leu
CA415076214
NM_005629.4:c.92C>T