Canonical Allele Identifier: PA2827947701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Lys2553Gln
CA338557
NM_001354895.2:c.7657A>C