Canonical Allele Identifier: PA2828007908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys1611Arg
CA16032947
NM_001354905.2:c.4832A>G