Allele Registry

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Canonical Allele Identifier: PA2828076528

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_001350049.1:p.Val53Leu	CA4938134 NM_001363120.2:c.157G>C CA372626214 NM_001363120.2:c.157G>T