Canonical Allele Identifier: PA2828048842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2501Phe
CA049365
NM_001354904.2:c.7502C>T