Canonical Allele Identifier: PA2827962521
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428129
ClinVar RCV Id: RCV000491729 RCV003651933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His2601Asp
CA16038213
NM_001354897.2:c.7801C>G