Canonical Allele Identifier: PA2827964202
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1764696
ClinVar RCV Id: RCV002373690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser268Arg
CA16023234
NM_001354898.2:c.802A>C
CA16023240
NM_001354898.2:c.804T>A
CA16023241
NM_001354898.2:c.804T>G