Canonical Allele Identifier: PA2827957297
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1027Ser
CA16028012
NM_001354897.2:c.3080A>G