Canonical Allele Identifier: PA2827980797
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2586969
ClinVar RCV Id: RCV003358454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2553Arg
CA16038140
NM_001354899.2:c.7657A>C
CA16038146
NM_001354899.2:c.7659T>A
CA16038147
NM_001354899.2:c.7659T>G