Canonical Allele Identifier: PA645463515
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 392671
ClinVar RCV Id: RCV000433087 RCV002305486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Asp16Glu
CA16609138
NM_005629.4:c.48C>A
CA415076017
NM_005629.4:c.48C>G