Canonical Allele Identifier: PA2827998982
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350422
ClinVar RCV Id: RCV000276968 RCV000462798 RCV000566206 RCV001712147 RCV003650574 RCV001731621 RCV003912493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2535Cys
CA049176
NM_001354901.2:c.7604C>G