Canonical Allele Identifier: PA2827977888
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp1670Asn
CA040634
NM_001354899.2:c.5008G>A