Canonical Allele Identifier: PA2826500620
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12073
ClinVar RCV Id: RCV000012854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254483.1:p.Asn33Asp
CA256458253
NM_001267554.1:c.97A>G