Canonical Allele Identifier: PA2827986964
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1657Asn
CA040634
NM_001354900.2:c.4969G>A