Canonical Allele Identifier: PA2825018747
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1108Lys
CA16028623
NM_000038.6:c.3324T>A
CA16028624
NM_000038.6:c.3324T>G