Canonical Allele Identifier: PA2827955250
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser306Asn
CA16023257
NM_001354897.2:c.917G>A