Canonical Allele Identifier: PA2828041719
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro1508Leu
CA040139
NM_001354904.2:c.4523C>T