Canonical Allele Identifier: PA2827960997
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2145Val
CA044550
NM_001354897.2:c.6433A>G