Canonical Allele Identifier: PA2828077306
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 473206
ClinVar RCV Id: RCV000537155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350051.1:p.Met21Ile
CA4938078
NM_001363122.2:c.63G>T
CA372625705
NM_001363122.2:c.63G>A
CA372625708
NM_001363122.2:c.63G>C