Canonical Allele Identifier: PA2828374940
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 142
ClinVar RCV Id: RCV000000165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Phe224Leu
CA339795
NM_001370085.1:c.670T>C
CA407963344
NM_001370085.1:c.672C>G
CA407963345
NM_001370085.1:c.672C>A