Canonical Allele Identifier: PA2741810367
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3063723
ClinVar RCV Id: RCV003988311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ser553Cys
CA414911812
NM_000132.4:c.1658C>G