Canonical Allele Identifier: PA2827989819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039868
ClinVar RCV Id: RCV002242334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Trp2523Cys
CA16038038
NM_001354900.2:c.7569G>C
CA16038039
NM_001354900.2:c.7569G>T