Canonical Allele Identifier: PA2828022986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 429050
ClinVar RCV Id: RCV000494666 RCV004003476 RCV003766766
ClinVar Variation Id: 2567044
ClinVar RCV Id: RCV003278306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1384Lys
CA16032274
NM_001354906.2:c.4152T>A
CA16032275
NM_001354906.2:c.4152T>G