Canonical Allele Identifier: PA2827967480
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val1295Glu
CA037191
NM_001354898.2:c.3884T>A