Canonical Allele Identifier: PA2825643790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1756303
ClinVar RCV Id: RCV002378152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg2301Ser
CA16036505
NM_001127511.3:c.6903A>C
CA16036506
NM_001127511.3:c.6903A>T