Canonical Allele Identifier: PA2825638892
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_001120983.2:p.Asp721Glu
CA16026191
NM_001127511.3:c.2163T>A
CA16026192
NM_001127511.3:c.2163T>G