Canonical Allele Identifier: PA2827993824
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn967Ser
CA16028071
NM_001354901.2:c.2900A>G