Canonical Allele Identifier: PA2827961799
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 851893
ClinVar RCV Id: RCV001776112 RCV002374932 RCV003649347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln2385His
CA16036850
NM_001354897.2:c.7155A>C
CA16036851
NM_001354897.2:c.7155A>T