Canonical Allele Identifier: PA2825024677
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2555Leu
CA16037984
NM_000038.6:c.7664C>T