Canonical Allele Identifier: PA2829904368
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2540360
ClinVar RCV Id: RCV003271732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062562.1:p.Val273Asp
CA7060157
NM_019616.4:c.818T>A