Canonical Allele Identifier: PA645396579
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371851
ClinVar RCV Id: RCV000410042 RCV002465647 RCV003418089 RCV003535698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser24Phe
CA059369
NM_001127511.3:c.71C>T