Canonical Allele Identifier: PA2827989779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys2512Gln
CA338557
NM_001354900.2:c.7534A>C