Canonical Allele Identifier: PA1139741861
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 964392
ClinVar RCV Id: RCV003652079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu2600Lys
CA16038148
NM_001354896.2:c.7798G>A