Canonical Allele Identifier: PA2829907296
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 368116
ClinVar RCV Id: RCV000292116 RCV002481262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Thr156Ala
CA10567753
NM_019863.3:c.466A>G