Canonical Allele Identifier: PA2825626568
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1739989
ClinVar RCV Id: RCV002332326 RCV003743953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile391Ser
CA16023873
NM_001127510.3:c.1172T>G