Canonical Allele Identifier: PA347011
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 210038
ClinVar RCV Id: RCV000191983 RCV001266471 RCV001778780
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240745.1:p.Ser128Leu
CA347010
NM_001253816.2:c.383C>T