Canonical Allele Identifier: PA2828012845
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2586969
ClinVar RCV Id: RCV003358454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2421Arg
CA16038140
NM_001354905.2:c.7261A>C
CA16038146
NM_001354905.2:c.7263T>A
CA16038147
NM_001354905.2:c.7263T>G