Canonical Allele Identifier: PA916042670
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_001341835.1:p.His927Tyr
CA008571
NM_001354906.2:c.2779C>T