Canonical Allele Identifier: PA2827971924
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly2647Val
CA16038743
NM_001354898.2:c.7940G>T