Canonical Allele Identifier: PA2827962455
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2583Val
CA013990
NM_001354897.2:c.7747A>G