Canonical Allele Identifier: PA2825024713
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039868
ClinVar RCV Id: RCV002242334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Trp2564Cys
CA16038038
NM_000038.6:c.7692G>C
CA16038039
NM_000038.6:c.7692G>T