Canonical Allele Identifier: PA2825012141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg71His
CA030877
NM_000038.6:c.212G>A