Canonical Allele Identifier: PA645399952
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233890
ClinVar RCV Id: RCV000223239 RCV000522947 RCV003743680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1380Ile
CA10578369
NM_001127510.3:c.4139C>T