Canonical Allele Identifier: PA2826733190
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 802660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274103.1:p.Pro201Leu
CA379779280
NM_001287174.3:c.602C>T