Canonical Allele Identifier: PA167749
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142204
ClinVar RCV Id: RCV000131194 RCV003764869 RCV003998089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg1040Trp
CA008046
NM_000038.6:c.3118A>T