Canonical Allele Identifier: PA2828029164
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2321Lys
CA10578451
NM_001354906.2:c.6963C>G
CA16038303
NM_001354906.2:c.6963C>A