Canonical Allele Identifier: PA2827955089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411395
ClinVar RCV Id: RCV000570604 RCV001174654 RCV002230492 RCV004001935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His260Arg
CA16022971
NM_001354897.2:c.779A>G