Canonical Allele Identifier: PA916030961
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 434042
ClinVar RCV Id: RCV000503292 RCV003313086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Arg1552Cys
CA5902425
NM_001351295.2:c.4654C>T