Canonical Allele Identifier: PA2827980743
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039868
ClinVar RCV Id: RCV002242334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Trp2536Cys
CA16038038
NM_001354899.2:c.7608G>C
CA16038039
NM_001354899.2:c.7608G>T