Canonical Allele Identifier: PA164032
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135698
ClinVar RCV Id: RCV000129238 RCV001357972 RCV003997376 RCV002515908 RCV003534356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His1210Tyr
CA008571
NM_000038.6:c.3628C>T