Canonical Allele Identifier: PA2828076596
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517510
ClinVar RCV Id: RCV002041103
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Pro134Ser
CA372627077
NM_001363120.2:c.400C>T