Canonical Allele Identifier: PA2826500814
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 420160
ClinVar RCV Id: RCV000482463 RCV001095705 RCV003313784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254483.1:p.Thr300Met
CA7060229
NM_001267554.1:c.899C>T