Canonical Allele Identifier: PA2825014122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His298Tyr
CA16023269
NM_000038.6:c.892C>T