Canonical Allele Identifier: PA2827975924
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1080Lys
CA16028623
NM_001354899.2:c.3240T>A
CA16028624
NM_001354899.2:c.3240T>G