Canonical Allele Identifier: PA2825639729
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 934037
ClinVar RCV Id: RCV003650659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly1001Arg
CA16028023
NM_001127511.3:c.3001G>A
CA16028024
NM_001127511.3:c.3001G>C