Canonical Allele Identifier: PA2827958341
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val1330Glu
CA037191
NM_001354897.2:c.3989T>A