Canonical Allele Identifier: PA297906
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819
ClinVar RCV Id: RCV000159571 RCV000573375 RCV000590001 RCV002516417 RCV003998421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2422Ala
CA012961
NM_000038.6:c.7264A>G