Canonical Allele Identifier: PA645294602
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_000123.1:p.Gln2208Arg
CA10567784
NM_000132.4:c.6623A>G