Canonical Allele Identifier: PA2828048376
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2443Arg
CA16038066
NM_001354904.2:c.7327A>C
CA16038072
NM_001354904.2:c.7329T>A
CA16038073
NM_001354904.2:c.7329T>G