Canonical Allele Identifier: PA2825644535
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039868
ClinVar RCV Id: RCV002242334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Trp2546Cys
CA16038038
NM_001127511.3:c.7638G>C
CA16038039
NM_001127511.3:c.7638G>T