Canonical Allele Identifier: PA2827954329
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133506
ClinVar RCV Id: RCV000120010 RCV000542057 RCV001705881 RCV003743571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser40Thr
CA023283
NM_001354897.2:c.119G>C