Allele Registry

Canonical Allele Identifier: PA120509

Gene: CHIT1 HGNC NCBI

ClinVar RCV:

RCV000010134

RCV000675725

ClinVar Variation:

9526

HGVS (amino-acid)	Matching Registered Transcripts
NP_003456.1:p.Gly102Ser	CA120508 NM_003465.3:c.304G>A