Canonical Allele Identifier: PA16039980
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233211
ClinVar RCV Id: RCV000219554 RCV003743670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1570Glu
CA10578381
NM_000038.6:c.4710T>A
CA16031660
NM_000038.6:c.4710T>G