Canonical Allele Identifier: PA2825016469
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 923027
ClinVar Variation Id: 1909279
ClinVar RCV Id: RCV003776606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp739Glu
CA16026191
NM_000038.6:c.2217T>A
CA16026192
NM_000038.6:c.2217T>G