Canonical Allele Identifier: PA117968
Gene: SLC33A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6132
ClinVar RCV Id: RCV000006506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004724.1:p.Ser113Arg
CA117967
NM_004733.3:c.339T>G
CA355143838
NM_004733.3:c.339T>A
CA355143842
NM_004733.3:c.337A>C