Canonical Allele Identifier: PA2827989986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760901
ClinVar RCV Id: RCV002412214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn2577Thr
CA16038395
NM_001354900.2:c.7730A>C