Canonical Allele Identifier: PA2827959577
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1708Asn
CA040634
NM_001354897.2:c.5122G>A