Canonical Allele Identifier: PA355915
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1108Ser
CA035035
NM_000038.6:c.3323A>G