Canonical Allele Identifier: PA2827973852
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro420Ala
CA027206
NM_001354899.2:c.1258C>G