Canonical Allele Identifier: PA2827962291
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2532Arg
CA16037774
NM_001354897.2:c.7595C>G