Canonical Allele Identifier: PA346988
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Pro319Ser
CA346987
NM_033409.4:c.955C>T