Canonical Allele Identifier: PA103785
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12085
ClinVar RCV Id: RCV000012866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Cys389Gly
CA121860
NM_000131.4:c.1165T>G