Canonical Allele Identifier: PA2825641075
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411562
ClinVar Variation Id: 941479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gln1426His
CA038623
NM_001127511.3:c.4278A>C
CA16030825
NM_001127511.3:c.4278A>T