Canonical Allele Identifier: PA2827977884
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1669Ala
CA10578392
NM_001354899.2:c.5005A>G