Canonical Allele Identifier: PA2828006776
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_001341831.1:p.Ser696Gly
CA031761
NM_001354902.2:c.2086A>G