Canonical Allele Identifier: PA2741815837
Gene: F12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2723904
ClinVar RCV Id: RCV003561523 RCV004555673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000496.2:p.Ser308Thr
CA3581346
NM_000505.4:c.922T>A