Canonical Allele Identifier: PA645387128
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 311270
ClinVar RCV Id: RCV000368932 RCV000881749
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Gln30His
CA7060350
NM_000504.4:c.90G>C
CA388787437
NM_000504.4:c.90G>T