Canonical Allele Identifier: PA2827977791
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1639Asp
CA040350
NM_001354899.2:c.4915A>G