Canonical Allele Identifier: PA2826733963
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576198
ClinVar RCV Id: RCV003322259 RCV003561296 RCV003466059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Pro1360Leu
CA5902590
NM_001287174.3:c.4079C>T