Canonical Allele Identifier: PA645294710
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 367997
ClinVar RCV Id: RCV000291239 RCV001080823 RCV002282128 RCV003389717 RCV002488831 RCV003970084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Ile7Phe
CA10529708
NM_000133.4:c.19A>T