Canonical Allele Identifier: PA2827606146
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_001338226.1:p.Pro1358Leu
CA5902590
NM_001351297.2:c.4073C>T