Canonical Allele Identifier: PA2827604899
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_001338225.1:p.Lys1336Asn
CA5902598
NM_001351296.2:c.4008G>C
CA379791157
NM_001351296.2:c.4008G>T