Canonical Allele Identifier: PA2828076999
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 210038
ClinVar RCV Id: RCV000191983 RCV001266471 RCV001778780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350050.1:p.Ser128Leu
CA347010
NM_001363121.2:c.383C>T