Canonical Allele Identifier: PA2827984713
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp975Val
CA16028005
NM_001354900.2:c.2924A>T