Canonical Allele Identifier: PA2826943700
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 626926
ClinVar RCV Id: RCV000851588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299603.1:p.Gly406Arg
CA388794353
NM_001312674.2:c.1216G>A
CA388794355
NM_001312674.2:c.1216G>C