Canonical Allele Identifier: PA2826943703
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098486
ClinVar RCV Id: RCV001420419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299603.1:p.Asp419His
CA388794502
NM_001312674.2:c.1255G>C