Canonical Allele Identifier: PA2828001486
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp967Gly
CA008117
NM_001354902.2:c.2900A>G