Canonical Allele Identifier: PA2828009145
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1832Ala
CA16034411
NM_001354905.2:c.5494C>G