Canonical Allele Identifier: PA2827959661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly1731Asp
CA10578397
NM_001354897.2:c.5192G>A