Canonical Allele Identifier: PA2827984722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489434
ClinVar RCV Id: RCV000580480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp977His
CA16028016
NM_001354900.2:c.2929G>C