Allele Registry

Canonical Allele Identifier: PA2580128678

Gene: CST9 HGNC NCBI

ClinVar RCV:

RCV004245570

ClinVar Variation:

2410581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008693.2:p.Arg78Ser	CA9790079 NM_001008693.3:c.234G>C CA408425078 NM_001008693.3:c.234G>T