Canonical Allele Identifier: PA1139752645
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956139
ClinVar RCV Id: RCV001228886 RCV002563153
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Arg275Cys
CA4938285
NM_024531.5:c.823C>T