Canonical Allele Identifier: PA16039997
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236610
ClinVar RCV Id: RCV000233240 RCV000590193 RCV000567766 RCV002487042 RCV003650527 RCV003998672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1655Ala
CA10582320
NM_000038.6:c.4963A>G