Canonical Allele Identifier: PA2827966750
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1083Ser
CA035035
NM_001354898.2:c.3248A>G