Canonical Allele Identifier: PA297897
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181817
ClinVar RCV Id: RCV000159569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn2405Ser
CA012942
NM_001127510.3:c.7214A>G