Canonical Allele Identifier: PA339479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216153
ClinVar RCV Id: RCV000200684 RCV000484738 RCV000575021 RCV000657015 RCV003316109 RCV003996966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala697Val
CA030702
NM_000038.6:c.2090C>T