Canonical Allele Identifier: PA2828374862
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 639327
ClinVar RCV Id: RCV000792095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Leu109Phe
CA407964066
NM_001370085.1:c.327G>C
CA407964067
NM_001370085.1:c.327G>T