Canonical Allele Identifier: PA16040007
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230437
ClinVar RCV Id: RCV000220073 RCV000708969 RCV003997837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1698Asn
CA040634
NM_000038.6:c.5092G>A