Canonical Allele Identifier: PA2827953446
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2691Ser
CA16038748
NM_001354896.2:c.8073A>C
CA16038749
NM_001354896.2:c.8073A>T