Canonical Allele Identifier: PA2825643048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2068Ala
CA044235
NM_001127511.3:c.6202C>G