Allele Registry

Canonical Allele Identifier: PA2580459181

Gene: CENPH HGNC NCBI

ClinVar RCV:

RCV004208171

ClinVar Variation:

2373181

HGVS (amino-acid)	Matching Registered Transcripts
NP_075060.1:p.Met7Arg	CA3291594 NM_022909.4:c.20T>G