Canonical Allele Identifier: PA168434
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_001120982.1:p.Ile2083Met
CA011046
NM_001127510.3:c.6249A>G