Canonical Allele Identifier: PA2827606281
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_001338226.1:p.Asp1470Asn
CA274147
NM_001351297.2:c.4408G>A