Canonical Allele Identifier: PA2828041922
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_001341833.1:p.Thr1529Ala
CA10582320
NM_001354904.2:c.4585A>G