Canonical Allele Identifier: PA2827955865
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2748653
ClinVar RCV Id: RCV003536633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser556Gly
CA16024881
NM_001354897.2:c.1666A>G
CA2697546184
NM_001354897.2:c.1665_1666delinsAG