Canonical Allele Identifier: PA2828010305
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1901Ala
CA16034411
NM_001354902.2:c.5701C>G