Canonical Allele Identifier: PA2827971430
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2497Arg
CA16037774
NM_001354898.2:c.7490C>G