Canonical Allele Identifier: PA2828029206
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566989
ClinVar RCV Id: RCV003278282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.His2490Asn
CA16038212
NM_001354903.2:c.7468C>A