Canonical Allele Identifier: PA916041967
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp469Gly
CA16024318
NM_001354897.2:c.1406A>G