Canonical Allele Identifier: PA658660357
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470051
ClinVar RCV Id: RCV000606972 RCV000566022 RCV002527852 RCV003128660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly2171Glu
CA045165
NM_001127510.3:c.6512G>A