Canonical Allele Identifier: PA2828076589
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006486
ClinVar RCV Id: RCV001303535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Ala124Val
CA4938176
NM_001363120.2:c.371C>T