Canonical Allele Identifier: PA113728
Gene: SLC1A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 9441
ClinVar RCV Id: RCV000010048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004163.3:p.Pro290Arg
CA254816
NM_004172.5:c.869C>G