Canonical Allele Identifier: PA2827960839
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466
ClinVar RCV Id: RCV000131598 RCV000759439 RCV002512548 RCV003534388 RCV003998112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2093Met
CA011046
NM_001354897.2:c.6279A>G