Canonical Allele Identifier: PA2828077382
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96703
ClinVar RCV Id: RCV000082865
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350051.1:p.Tyr141Cys
CA345438
NM_001363122.2:c.422A>G