Canonical Allele Identifier: PA2825636975
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1428880
ClinVar RCV Id: RCV003653529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Trp50Cys
CA360612167
NM_001127511.3:c.150G>C
CA360612169
NM_001127511.3:c.150G>T