Canonical Allele Identifier: PA2827983267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 656514
ClinVar RCV Id: RCV003653381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Leu507Met
CA16024894
NM_001354900.2:c.1519T>A