Canonical Allele Identifier: PA2825024783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2586969
ClinVar RCV Id: RCV003358454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2581Arg
CA16038140
NM_000038.6:c.7741A>C
CA16038146
NM_000038.6:c.7743T>A
CA16038147
NM_000038.6:c.7743T>G