Canonical Allele Identifier: PA2828009103
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1826Leu
CA043504
NM_001354905.2:c.5477C>T