Canonical Allele Identifier: PA2827998895
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2510Arg
CA16038066
NM_001354901.2:c.7528A>C
CA16038072
NM_001354901.2:c.7530T>A
CA16038073
NM_001354901.2:c.7530T>G