Canonical Allele Identifier: PA2827957371
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727806
ClinVar RCV Id: RCV002320438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly1049Val
CA16028163
NM_001354897.2:c.3146G>T