Canonical Allele Identifier: PA2827960355
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro1944Leu
CA010706
NM_001354897.2:c.5831C>T