Canonical Allele Identifier: PA2825147632
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_000343.2:p.Phe198del
CA5903817
NM_000352.6:c.592_594del