Canonical Allele Identifier: PA2827940377
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452729
ClinVar RCV Id: RCV003177503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser294Cys
CA16023246
NM_001354895.2:c.881C>G