Canonical Allele Identifier: PA916041743
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482397
ClinVar RCV Id: RCV000573977 RCV003767148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2761Ser
CA050243
NM_001354896.2:c.8282A>G