Canonical Allele Identifier: PA103777
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 265135
ClinVar RCV Id: RCV000254994 RCV000714620 RCV002252070 RCV002280876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000122.1:p.Cys370Phe
CA7060222
NM_000131.4:c.1109G>T