Canonical Allele Identifier: PA1139668373
Gene: F12 HGNC NCBI

Linked Data

ClinVar Variation Id: 904494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000496.2:p.Gln319His
CA362328366
NM_000505.4:c.957G>C
CA362328368
NM_000505.4:c.957G>T