Canonical Allele Identifier: PA916041948
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val452Asp
CA16024206
NM_001354897.2:c.1355T>A