Canonical Allele Identifier: PA2825644569
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 918607
ClinVar RCV Id: RCV001176273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala2558Pro
CA16038109
NM_001127511.3:c.7672G>C