Canonical Allele Identifier: PA2828033284
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2748653
ClinVar RCV Id: RCV003536633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser420Gly
CA16024881
NM_001354904.2:c.1258A>G
CA2697546184
NM_001354904.2:c.1257_1258delinsAG