Canonical Allele Identifier: PA2580105362
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2477679
ClinVar RCV Id: RCV003204015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ala1993Ser
CA10567921
NM_000132.4:c.5977G>T