Canonical Allele Identifier: PA2827961794
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met2383Arg
CA16036833
NM_001354897.2:c.7148T>G