Canonical Allele Identifier: PA2828007077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Arg1480Trp
CA009806
NM_001354905.2:c.4438C>T