Canonical Allele Identifier: PA2827984398
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Leu881Phe
CA033363
NM_001354900.2:c.2641C>T