Canonical Allele Identifier: PA2826170102
Gene: SLC33A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469748
ClinVar RCV Id: RCV001995036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177921.1:p.Ser67Arg
CA2677439
NM_001190992.2:c.201C>G
CA355144162
NM_001190992.2:c.201C>A
CA355144170
NM_001190992.2:c.199A>C