Canonical Allele Identifier: PA2828007853
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1900687
ClinVar RCV Id: RCV003776566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1600Ser
CA16032868
NM_001354905.2:c.4798C>T