Canonical Allele Identifier: PA2828019697
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1017His
CA16028675
NM_001354903.2:c.3049A>C