Canonical Allele Identifier: PA2828000079
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2769012
ClinVar RCV Id: RCV003538221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu212Gln
CA16022659
NM_001354902.2:c.634G>C