Canonical Allele Identifier: PA916041533
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys2571Gln
CA338557
NM_001354896.2:c.7711A>C