Canonical Allele Identifier: PA2827980491
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2462Gly
CA16037580
NM_001354899.2:c.7385A>G