Canonical Allele Identifier: PA2828022892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1367Ser
CA040262
NM_001354906.2:c.4100A>G