Canonical Allele Identifier: PA2827962599
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1064027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2628Ile
CA16038397
NM_001354897.2:c.7883A>T