Canonical Allele Identifier: PA2827949969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186336
ClinVar RCV Id: RCV000165915 RCV003650426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His444Arg
CA004248
NM_001354896.2:c.1331A>G