Canonical Allele Identifier: PA2828046551
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411553
ClinVar RCV Id: RCV003766600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg2179Gly
CA16036410
NM_001354904.2:c.6535A>G