Allele Registry

Canonical Allele Identifier: PA645495767

Gene: ALMS1 HGNC NCBI

ClinVar Variation Id: 393372

HGVS (amino-acid)	Matching Registered Transcripts
NP_055935.4:p.Pro1389Leu	CA1713648 NM_015120.4:c.4166C>T