Canonical Allele Identifier: PA916030867
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_001338224.1:p.Asp901Asn
CA5903065
NM_001351295.2:c.2701G>A