Canonical Allele Identifier: PA2828000039
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469975
ClinVar RCV Id: RCV000567343 RCV001193497 RCV003537071 RCV003999396 RCV003332195
ClinVar Variation Id: 1499759
ClinVar RCV Id: RCV003745511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp166Glu
CA039593
NM_001354902.2:c.498C>G
CA16022345
NM_001354902.2:c.498C>A