Canonical Allele Identifier: PA2828015970
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2748653
ClinVar RCV Id: RCV003536633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser263Gly
CA16024881
NM_001354906.2:c.787A>G
CA2697546184
NM_001354906.2:c.786_787delinsAG