Canonical Allele Identifier: PA2828040857
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn1405His
CA16031385
NM_001354904.2:c.4213A>C