Canonical Allele Identifier: PA2828001432
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg949Trp
CA008046
NM_001354902.2:c.2845A>T