Canonical Allele Identifier: PA2828001570
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1027Ser
CA16028677
NM_001354902.2:c.3080A>G