Canonical Allele Identifier: PA189697
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile2573Val
CA013990
NM_000038.6:c.7717A>G