Canonical Allele Identifier: PA2827961540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2306Asn
CA16036358
NM_001354897.2:c.6917G>A