Canonical Allele Identifier: PA2827969977
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile2058Met
CA011046
NM_001354898.2:c.6174A>G