Canonical Allele Identifier: PA645398798
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419733
ClinVar RCV Id: RCV000478476 RCV000572352 RCV003409657 RCV003743736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr281Ala
CA050760
NM_001127510.3:c.841A>G