Canonical Allele Identifier: PA2573225491
Gene: SLC18A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1394695
ClinVar RCV Id: RCV001898601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003046.2:p.Ile61Met
CA5496703
NM_003055.3:c.183C>G