Canonical Allele Identifier: PA2827946158
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2086Ala
CA044235
NM_001354895.2:c.6256C>G