Canonical Allele Identifier: PA2827989749
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135719
ClinVar RCV Id: RCV000122802 RCV000235882 RCV000766452 RCV000575243 RCV003997387 RCV003534362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn2501Ser
CA013956
NM_001354900.2:c.7502A>G