Canonical Allele Identifier: PA2827999688
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2751Ser
CA015484
NM_001354901.2:c.8252A>G