Canonical Allele Identifier: PA2825017862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser970Asn
CA033901
NM_000038.6:c.2909G>A