Canonical Allele Identifier: PA645400255
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1755Val
CA041104
NM_001127510.3:c.5264C>T