Canonical Allele Identifier: PA2827978145
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1743Arg
CA16032947
NM_001354899.2:c.5228A>G