Canonical Allele Identifier: PA2826946979
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2636137
ClinVar RCV Id: RCV003402867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Glu248Asp
CA414444527
NM_001313913.2:c.744G>C
CA414444530
NM_001313913.2:c.744G>T