Canonical Allele Identifier: PA2825021919
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1843Thr
CA16033423
NM_000038.6:c.5527C>A