Canonical Allele Identifier: PA2827953662
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Tyr96Cys
CA033841
NM_001354896.2:c.287A>G