Canonical Allele Identifier: PA297689
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181776
ClinVar RCV Id: RCV000569152 RCV000679054 RCV003534397 RCV003998397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1017del
CA008002
NM_001127510.3:c.3049_3051del