Canonical Allele Identifier: PA2828007737
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1049Arg
CA16028829
NM_001354902.2:c.3146C>G