Canonical Allele Identifier: PA2828015139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.His298Tyr
CA16023269
NM_001354903.2:c.892C>T