Canonical Allele Identifier: PA2825852730
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 436771
ClinVar RCV Id: RCV000499651 RCV000640937 RCV001092998 RCV001834620 RCV002323868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Ala273Thr
CA10549443
NM_001142806.1:c.817G>A