Canonical Allele Identifier: PA915980627
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 465147
ClinVar RCV Id: RCV000713356 RCV001088436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Val67Met
CA10549204
NM_001142806.1:c.199G>A