Canonical Allele Identifier: PA2825645051
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1318535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala2712Asp
CA16039108
NM_001127511.3:c.8135C>A