Canonical Allele Identifier: PA2573202860
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600562
ClinVar RCV Id: RCV002132451 RCV002486899 RCV003025438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Pro658Leu
CA5903382
NM_001351295.2:c.1973C>T