Canonical Allele Identifier: PA2828013141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2467Phe
CA049365
NM_001354905.2:c.7400C>T