Canonical Allele Identifier: PA2828374895
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 844883
ClinVar RCV Id: RCV001047843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Gly162Val
CA407963739
NM_001370085.1:c.485G>T