Canonical Allele Identifier: PA2828052998
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 499832
ClinVar RCV Id: RCV000592962 RCV003160031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001344250.1:p.Leu602Val
CA1637670
NM_001357321.2:c.1804C>G