Canonical Allele Identifier: PA2825148794
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 551435
ClinVar RCV Id: RCV000666495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000343.2:p.Arg1418Leu
CA379786696
NM_000352.6:c.4253G>T