Canonical Allele Identifier: PA16039894
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly907Arg
CA033124
NM_000038.6:c.2719G>A
CA033134
NM_000038.6:c.2719G>C