Canonical Allele Identifier: PA2828013121
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2464Lys
CA16038436
NM_001354905.2:c.7392T>A
CA16038437
NM_001354905.2:c.7392T>G