Canonical Allele Identifier: PA297867
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181811
ClinVar RCV Id: RCV000167931 RCV000159563 RCV000491513 RCV003998416 RCV003534411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp2033Glu
CA010908
NM_001127510.3:c.6099C>G
CA16034682
NM_001127510.3:c.6099C>A