Canonical Allele Identifier: PA2827972449
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2806Leu
CA050906
NM_001354898.2:c.8417C>T