Canonical Allele Identifier: PA110441
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10607
ClinVar RCV Id: RCV000011353 RCV000792734 RCV000851963 RCV001810849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Thr342Met
CA255381
NM_000133.4:c.1025C>T