Canonical Allele Identifier: PA2827958771
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg1460Gln
CA009471
NM_001354897.2:c.4379G>A