Canonical Allele Identifier: PA2827974418
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 83212
ClinVar RCV Id: RCV000074203 RCV000573010 RCV001192945 RCV001854267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile610Val
CA006325
NM_001354899.2:c.1828A>G