Canonical Allele Identifier: PA2825635479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1318535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2730Asp
CA16039108
NM_001127510.3:c.8189C>A