Canonical Allele Identifier: PA2827962092
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569210
ClinVar RCV Id: RCV000776331 RCV003999536 RCV003478409 RCV003768055 RCV003492129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2474Cys
CA16037430
NM_001354897.2:c.7421C>G