Canonical Allele Identifier: PA2827606122
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 551087
ClinVar RCV Id: RCV000666053 RCV001816668 RCV001104230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338226.1:p.Lys1335Asn
CA5902598
NM_001351297.2:c.4005G>C
CA379791157
NM_001351297.2:c.4005G>T