Canonical Allele Identifier: PA2827981039
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761379
ClinVar RCV Id: RCV002412380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2625Asn
CA16038614
NM_001354899.2:c.7875A>C
CA16038615
NM_001354899.2:c.7875A>T