Canonical Allele Identifier: PA112536
Gene: PROS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1523041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000304.2:p.Pro667Leu
CA353669459
NM_000313.4:c.2000C>T
CA2573137476
NM_000313.4:c.2000_2001delinsTG