Canonical Allele Identifier: PA2827960719
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411334
ClinVar RCV Id: RCV000571749 RCV000733231 RCV003651838 RCV004001912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2054Asn
CA043925
NM_001354897.2:c.6161G>A