Canonical Allele Identifier: PA1139730208
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 550521
ClinVar RCV Id: RCV000665287 RCV002253545 RCV002253544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Phe198del
CA5903817
NM_001351297.2:c.592_594del