Canonical Allele Identifier: PA2827999764
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2772Leu
CA050906
NM_001354901.2:c.8315C>T