Canonical Allele Identifier: PA163792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135706
ClinVar RCV Id: RCV000122784 RCV000129088 RCV001157159 RCV000479916 RCV003389701 RCV003534358 RCV000587086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1696Asn
CA009886
NM_001127511.3:c.5086G>A