Canonical Allele Identifier: PA2828040137
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1319Ala
CA009444
NM_001354904.2:c.3955A>G