Canonical Allele Identifier: PA2827949988
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro448Ala
CA027206
NM_001354896.2:c.1342C>G