Canonical Allele Identifier: PA2827981765
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 821606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg29Leu
CA16021916
NM_001354900.2:c.86G>T