Canonical Allele Identifier: PA2827974161
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2748653
ClinVar RCV Id: RCV003536633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser518Gly
CA16024881
NM_001354899.2:c.1552A>G
CA2697546184
NM_001354899.2:c.1551_1552delinsAG