Canonical Allele Identifier: PA2825022848
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2086Ala
CA044235
NM_000038.6:c.6256C>G