Canonical Allele Identifier: PA2827604962
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338249
ClinVar RCV Id: RCV001822847 RCV003321873
ClinVar Variation Id: 2829734
ClinVar RCV Id: RCV003686414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338225.1:p.Gly1383Arg
CA5902549
NM_001351296.2:c.4147G>A
CA379788258
NM_001351296.2:c.4147G>C