Canonical Allele Identifier: PA2828007938
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1618Arg
CA16032991
NM_001354905.2:c.4853C>G