Canonical Allele Identifier: PA2825851991
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2727804
ClinVar RCV Id: RCV003513429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Pro50Gln
CA415076514
NM_001142805.2:c.149C>A