Canonical Allele Identifier: PA2828049101
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg2544Ile
CA16038731
NM_001354904.2:c.7631G>T