Canonical Allele Identifier: PA2827957688
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489437
ClinVar RCV Id: RCV000579783 RCV003767262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser1138Cys
CA035180
NM_001354897.2:c.3413C>G