Canonical Allele Identifier: PA2827962469
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala2586Thr
CA16038108
NM_001354897.2:c.7756G>A