Canonical Allele Identifier: PA2828007483
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233215
ClinVar Variation Id: 862543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser937Arg
CA10578350
NM_001354902.2:c.2811T>A
CA16028081
NM_001354902.2:c.2809A>C
CA16028087
NM_001354902.2:c.2811T>G