Canonical Allele Identifier: PA2827957331
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1036Thr
CA16028070
NM_001354897.2:c.3107A>C