Canonical Allele Identifier: PA2827964671
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val417Asp
CA16024206
NM_001354898.2:c.1250T>A