Canonical Allele Identifier: PA2825021199
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655826
ClinVar RCV Id: RCV003536010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu1663Asp
CA16032250
NM_000038.6:c.4989A>C
CA16032251
NM_000038.6:c.4989A>T