Canonical Allele Identifier: PA2828055617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn948Lys
CA16028623
NM_001354905.2:c.2844T>A
CA16028624
NM_001354905.2:c.2844T>G