Canonical Allele Identifier: PA2828003468
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1992Met
CA011046
NM_001354902.2:c.5976A>G