Canonical Allele Identifier: PA215536
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln2291His
CA012603
NM_001127510.3:c.6873A>T
CA16036332
NM_001127510.3:c.6873A>C