Canonical Allele Identifier: PA916030909
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 551087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Lys1358Asn
CA5902598
NM_001351295.2:c.4074G>C
CA379791157
NM_001351295.2:c.4074G>T