Canonical Allele Identifier: PA2827990627
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn2769Ser
CA015484
NM_001354900.2:c.8306A>G