Canonical Allele Identifier: PA2827979935
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1756303
ClinVar RCV Id: RCV002378152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg2291Ser
CA16036505
NM_001354899.2:c.6873A>C
CA16036506
NM_001354899.2:c.6873A>T