Canonical Allele Identifier: PA916030913
Gene: ABCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 549539
ClinVar RCV Id: RCV000664135 RCV002245072 RCV002245071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338224.1:p.Asn1370Ser
CA379790767
NM_001351295.2:c.4109A>G