Canonical Allele Identifier: PA2828048436
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile2447Val
CA013990
NM_001354904.2:c.7339A>G