Canonical Allele Identifier: PA2827966511
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg1015Trp
CA008046
NM_001354898.2:c.3043A>T