Canonical Allele Identifier: PA2827973677
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1510117
ClinVar RCV Id: RCV003745523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp369Ala
CA16023910
NM_001354899.2:c.1106A>C