Canonical Allele Identifier: PA2827959734
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg1752Leu
CA16032754
NM_001354897.2:c.5255G>T