Canonical Allele Identifier: PA2827968816
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1701Gly
CA009909
NM_001354898.2:c.5102A>G