Canonical Allele Identifier: PA645294916
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 291081
ClinVar RCV Id: RCV000383804 RCV000851679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Ala430Thr
CA3163944
NM_000128.4:c.1288G>A