Canonical Allele Identifier: PA2827957280
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2092648
ClinVar RCV Id: RCV003744871
ClinVar Variation Id: 2683854
ClinVar RCV Id: RCV003484463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1022Lys
CA16027973
NM_001354897.2:c.3066T>A
CA16027974
NM_001354897.2:c.3066T>G