Canonical Allele Identifier: PA2827962614
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 941683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2632Gln
CA1139659004
NM_001354897.2:c.7895_7896delinsAG