Canonical Allele Identifier: PA2825637942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys380Arg
CA026866
NM_001127511.3:c.1139A>G