Canonical Allele Identifier: PA2827989948
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn2563Lys
CA10578451
NM_001354900.2:c.7689C>G
CA16038303
NM_001354900.2:c.7689C>A