Canonical Allele Identifier: PA2827980752
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2541Arg
CA16038066
NM_001354899.2:c.7621A>C
CA16038072
NM_001354899.2:c.7623T>A
CA16038073
NM_001354899.2:c.7623T>G