Canonical Allele Identifier: PA2825022439
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630442
ClinVar RCV Id: RCV000775825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1981Thr
CA16034335
NM_000038.6:c.5942A>C