Canonical Allele Identifier: PA2828028990
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470102
ClinVar RCV Id: RCV002395426 RCV003742792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2454Leu
CA16037984
NM_001354903.2:c.7361C>T