Canonical Allele Identifier: PA2828046497
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2170Asn
CA16036358
NM_001354904.2:c.6509G>A