Canonical Allele Identifier: PA2825852726
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 533700
ClinVar RCV Id: RCV000640931 RCV001255373 RCV002251491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Pro267Leu
CA415086073
NM_001142806.1:c.800C>T