Canonical Allele Identifier: PA2828009752
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1687Arg
CA16032991
NM_001354902.2:c.5060C>G