Canonical Allele Identifier: PA2828030856
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2741Ala
CA015593
NM_001354903.2:c.8221T>G