Canonical Allele Identifier: PA2827962487
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2586969
ClinVar RCV Id: RCV003358454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2591Arg
CA16038140
NM_001354897.2:c.7771A>C
CA16038146
NM_001354897.2:c.7773T>A
CA16038147
NM_001354897.2:c.7773T>G