Canonical Allele Identifier: PA2827956148
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp661Gly
CA16025584
NM_001354897.2:c.1982A>G