Canonical Allele Identifier: PA2827984999
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1066Ser
CA16028614
NM_001354900.2:c.3196G>T