Canonical Allele Identifier: PA2827982925
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val383Asp
CA16024206
NM_001354900.2:c.1148T>A