Canonical Allele Identifier: PA2827962517
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566989
ClinVar RCV Id: RCV003278282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His2601Asn
CA16038212
NM_001354897.2:c.7801C>A