Canonical Allele Identifier: PA2827956735
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg855Cys
CA16026883
NM_001354897.2:c.2563C>T