Canonical Allele Identifier: PA1139671016
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 835343
ClinVar RCV Id: RCV001036203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Val419Met
CA414446878
NM_000133.4:c.1255G>A