Allele Registry

Canonical Allele Identifier: PA3057491983

Gene: F8 HGNC NCBI

ClinVar Allele:

3729685

ClinVar RCV:

RCV005041718

ClinVar Variation:

3598201

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Thr38Ser	CA414907336 NM_019863.3:c.113C>G CA414907345 NM_019863.3:c.112A>T