Canonical Allele Identifier: PA2828010276
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1895Leu
CA043504
NM_001354902.2:c.5684C>T