Canonical Allele Identifier: PA2827950737
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133525
ClinVar RCV Id: RCV000120035 RCV001775597 RCV000568678 RCV004019666 RCV003534351 RCV003997331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1021Asn
CA007992
NM_001354896.2:c.3061G>A