Canonical Allele Identifier: PA2828022465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile1456Asn
CA16031568
NM_001354903.2:c.4367T>A