Canonical Allele Identifier: PA915958279
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 811121
ClinVar RCV Id: RCV001000773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Lys126Arg
CA414919889
NM_000132.4:c.377A>G