Canonical Allele Identifier: PA2827989776
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2511Cys
CA16037960
NM_001354900.2:c.7531A>T