Canonical Allele Identifier: PA2827990548
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn2744His
CA050563
NM_001354900.2:c.8230A>C