Canonical Allele Identifier: PA2828017060
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Tyr454His
CA031174
NM_001354906.2:c.1360T>C