Canonical Allele Identifier: PA2825014981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 937461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln445His
CA16024227
NM_000038.6:c.1335G>C
CA16024228
NM_000038.6:c.1335G>T