Canonical Allele Identifier: PA2827966475
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233215
ClinVar Variation Id: 862543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1003Arg
CA10578350
NM_001354898.2:c.3009T>A
CA16028081
NM_001354898.2:c.3007A>C
CA16028087
NM_001354898.2:c.3009T>G