Canonical Allele Identifier: PA167843
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142240
ClinVar RCV Id: RCV000131243 RCV000230602 RCV000758727 RCV003998093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg1051Gly
CA008168
NM_001127511.3:c.3151A>G