Canonical Allele Identifier: PA274148
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 188931
ClinVar RCV Id: RCV000169299 RCV000586940 RCV001277177 RCV001385864 RCV003468839 RCV004545752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Asp1472Asn
CA274147
NM_001287174.3:c.4414G>A