Canonical Allele Identifier: PA2827957359
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469907
ClinVar RCV Id: RCV003742670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Glu1044Val
CA16028127
NM_001354897.2:c.3131A>T