Canonical Allele Identifier: PA2827472168
Gene: SLCO1B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2511599
ClinVar RCV Id: RCV004284477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336849.1:p.Gly70Arg
CA6475127
NM_001349920.2:c.208G>C
CA384098993
NM_001349920.2:c.208G>A