Canonical Allele Identifier: PA2825644615
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His2573Pro
CA049129
NM_001127511.3:c.7718A>C