Canonical Allele Identifier: PA645396592
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371861
ClinVar RCV Id: RCV000409742 RCV003892008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly42Asp
CA16042081
NM_001127511.3:c.125G>A