Canonical Allele Identifier: PA2827991892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu350Ile
CA16023982
NM_001354901.2:c.1048C>A