Canonical Allele Identifier: PA916039887
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428135
ClinVar RCV Id: RCV000491956 RCV000677765 RCV002465690 RCV001775829 RCV004003444 RCV002523433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser861Gly
CA032383
NM_001354896.2:c.2581A>G