Canonical Allele Identifier: PA097320
Gene: F12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1168
ClinVar RCV Id: RCV000778921 RCV001158012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000496.2:p.Tyr53Cys
CA114815
NM_000505.4:c.158A>G