Canonical Allele Identifier: PA2827942642
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn1026Ser
CA16028071
NM_001354895.2:c.3077A>G