Canonical Allele Identifier: PA211752
Gene: PROS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161353
ClinVar RCV Id: RCV000148759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000304.2:p.Cys226Ser
CA211751
NM_000313.4:c.676T>A
CA353673177
NM_000313.4:c.677G>C