Canonical Allele Identifier: PA658660349
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 449370
ClinVar RCV Id: RCV000519065 RCV000851605 RCV003403227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Glu200Gly
CA10568575
NM_000132.4:c.599A>G