Canonical Allele Identifier: PA2827989676
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677520
ClinVar RCV Id: RCV003471656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg2480Ser
CA16037770
NM_001354900.2:c.7440A>C
CA16037771
NM_001354900.2:c.7440A>T