Canonical Allele Identifier: PA2827980593
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927392
ClinVar RCV Id: RCV001190627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2490Ser
CA048409
NM_001354899.2:c.7469A>G