Canonical Allele Identifier: PA2825018821
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1118Ser
CA16028677
NM_000038.6:c.3353A>G