Canonical Allele Identifier: PA2827966455
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp991Val
CA16028005
NM_001354898.2:c.2972A>T