Canonical Allele Identifier: PA2828053017
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1781250
ClinVar RCV Id: RCV002412937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001344250.1:p.Pro615Ser
CA1637682
NM_001357321.2:c.1843C>T