Canonical Allele Identifier: PA2825640039
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1100His
CA16028675
NM_001127511.3:c.3298A>C