Canonical Allele Identifier: PA2827972788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Tyr96Cys
CA033841
NM_001354899.2:c.287A>G