Canonical Allele Identifier: PA346968
Gene: SLC52A3 HGNC NCBI
ClinVar RCV:
RCV000191956
ClinVar Variation:
210011
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Trp17Arg
CA346967
NM_033409.4:c.49T>C
CA407964647
NM_033409.4:c.49T>A