Canonical Allele Identifier: PA658659426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744
ClinVar RCV Id: RCV003470761 RCV000566086 RCV003999368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser787Gly
CA031761
NM_001127510.3:c.2359A>G