Canonical Allele Identifier: PA2827955538
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2102478
ClinVar RCV Id: RCV003744899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile414Val
CA16023953
NM_001354897.2:c.1240A>G