Canonical Allele Identifier: PA2827965259
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127279
ClinVar RCV Id: RCV000115071
ClinVar Variation Id: 628655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile613Leu
CA006331
NM_001354898.2:c.1837A>T
CA16025497
NM_001354898.2:c.1837A>C