Canonical Allele Identifier: PA2828011487
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 857579
ClinVar RCV Id: RCV003649364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met2213Lys
CA16036831
NM_001354905.2:c.6638T>A