Canonical Allele Identifier: PA658686832
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_001120982.1:p.Ser1128Cys
CA035180
NM_001127510.3:c.3383C>G