Canonical Allele Identifier: PA2827942659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1721460
ClinVar RCV Id: RCV003743922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Lys1030Asn
CA16028099
NM_001354895.2:c.3090A>C
CA16028100
NM_001354895.2:c.3090A>T