Canonical Allele Identifier: PA645440891
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 336086
ClinVar RCV Id: RCV000367511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071882.1:p.Ala559Ser
CA10615481
NM_022437.3:c.1675G>T