Canonical Allele Identifier: PA2828048661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2478Lys
CA10578451
NM_001354904.2:c.7434C>G
CA16038303
NM_001354904.2:c.7434C>A