Canonical Allele Identifier: PA2826362052
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423007
ClinVar RCV Id: RCV001926407
ClinVar Variation Id: 2415988
ClinVar RCV Id: RCV003105200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240745.1:p.Val53Leu
CA4938134
NM_001253816.2:c.157G>C
CA372626214
NM_001253816.2:c.157G>T