Canonical Allele Identifier: PA16039893
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811
ClinVar RCV Id: RCV000220564 RCV002515681 RCV003743663 RCV003998003 RCV003477749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met891Thr
CA10578343
NM_000038.6:c.2672T>C