Canonical Allele Identifier: PA2825014677
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His392Tyr
CA16023877
NM_000038.6:c.1174C>T