Canonical Allele Identifier: PA2827966454
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1315725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp991Tyr
CA16028002
NM_001354898.2:c.2971G>T