Canonical Allele Identifier: PA2827951096
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1136Ser
CA16028677
NM_001354896.2:c.3407A>G