Canonical Allele Identifier: PA2827957444
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1068Gly
CA008117
NM_001354897.2:c.3203A>G