Canonical Allele Identifier: PA2826210776
Gene: SLC1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1362190
ClinVar RCV Id: RCV001900057 RCV002548735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182657.1:p.Cys554Ser
CA5946995
NM_001195728.3:c.1660T>A
CA380124725
NM_001195728.3:c.1661G>C