Canonical Allele Identifier: PA2827971687
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1343462
ClinVar Variation Id: 1378873
ClinVar RCV Id: RCV003745382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2576Arg
CA16038274
NM_001354898.2:c.7726A>C
CA16038280
NM_001354898.2:c.7728T>A
CA16038281
NM_001354898.2:c.7728T>G