Canonical Allele Identifier: PA916071865
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 368117
ClinVar RCV Id: RCV000403190 RCV002252106 RCV003392221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Gln73Arg
CA10567784
NM_019863.3:c.218A>G