Canonical Allele Identifier: PA2827991069
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141928
ClinVar RCV Id: RCV000130643 RCV000148370 RCV000211892 RCV000206082 RCV000656744 RCV003998072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys91Arg
CA009591
NM_001354901.2:c.272A>G