Canonical Allele Identifier: PA2827962278
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Tyr2527Cys
CA013809
NM_001354897.2:c.7580A>G