Canonical Allele Identifier: PA2827949971
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411398
ClinVar RCV Id: RCV003651853 RCV002383828
ClinVar Variation Id: 485101
ClinVar RCV Id: RCV000563421 RCV003767208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His444Gln
CA027188
NM_001354896.2:c.1332T>G
CA16024222
NM_001354896.2:c.1332T>A