Canonical Allele Identifier: PA2825629756
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2061927
ClinVar RCV Id: RCV003534916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1033His
CA16028116
NM_001127510.3:c.3097G>C