Canonical Allele Identifier: PA2827985002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1067Ser
CA035035
NM_001354900.2:c.3200A>G