Canonical Allele Identifier: PA2499252506
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn982Lys
CA16028623
NM_001354904.2:c.2946T>A
CA16028624
NM_001354904.2:c.2946T>G