Canonical Allele Identifier: PA916042141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 826163
ClinVar RCV Id: RCV001024848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu212Val
CA16022663
NM_001354902.2:c.635A>T