Canonical Allele Identifier: PA2827605790
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 303771
ClinVar RCV Id: RCV000290773 RCV000331715 RCV000386179 RCV001820892 RCV002520700 RCV002480109 RCV002520699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Asp878Asn
CA5903065
NM_001351297.2:c.2632G>A