Canonical Allele Identifier: PA2825014089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 938897
ClinVar RCV Id: RCV003650680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser294Ala
CA16023244
NM_000038.6:c.880T>G