Canonical Allele Identifier: PA16040133
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His255Arg
CA048853
NM_000038.6:c.764A>G