Canonical Allele Identifier: PA916040443
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266
ClinVar RCV Id: RCV000565169 RCV001805192 RCV002530260 RCV003409840 RCV003651988 RCV004000951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1652Leu
CA040139
NM_001354896.2:c.4955C>T