Canonical Allele Identifier: PA097293
Gene: F12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1170
ClinVar RCV Id: RCV000001229 RCV000414902 RCV001198361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000496.2:p.Thr328Arg
CA114819
NM_000505.4:c.983C>G