Canonical Allele Identifier: PA2827606349
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2994775
ClinVar RCV Id: RCV003858398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Thr1533Asn
CA379781795
NM_001351297.2:c.4598C>A