Canonical Allele Identifier: PA2826361673
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642607
ClinVar RCV Id: RCV000796101
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240744.1:p.Pro73Ser
CA4938144
NM_001253815.2:c.217C>T