Canonical Allele Identifier: PA2828012108
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2406Trp
CA16037624
NM_001354902.2:c.7217C>G