Canonical Allele Identifier: PA916030979
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 9110
ClinVar RCV Id: RCV000009680 RCV002512948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Pro45Leu
CA254640
NM_001351297.2:c.134C>T