Canonical Allele Identifier: PA2825644546
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2551Arg
CA16038066
NM_001127511.3:c.7651A>C
CA16038072
NM_001127511.3:c.7653T>A
CA16038073
NM_001127511.3:c.7653T>G