Canonical Allele Identifier: PA916021189
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 311270
ClinVar RCV Id: RCV000368932 RCV000881749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299604.1:p.Gln30His
CA7060350
NM_001312675.2:c.90G>C
CA388787437
NM_001312675.2:c.90G>T