Canonical Allele Identifier: PA286694
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127325
ClinVar RCV Id: RCV000115128 RCV000197863 RCV000590250 RCV000722129 RCV003534346 RCV003997232 RCV003952546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2736Asn
CA014491
NM_001127511.3:c.8207G>A