Canonical Allele Identifier: PA2828015091
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368407
ClinVar RCV Id: RCV003772579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser290Arg
CA16023216
NM_001354903.2:c.868A>C
CA16023221
NM_001354903.2:c.870T>A
CA16023222
NM_001354903.2:c.870T>G