Canonical Allele Identifier: PA2828046786
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2214His
CA046653
NM_001354904.2:c.6640A>C