Canonical Allele Identifier: PA2827981063
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1932430
ClinVar RCV Id: RCV002605780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu2634Val
CA16038674
NM_001354899.2:c.7901A>T