Canonical Allele Identifier: PA645495958
Gene: ALMS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 434131
ClinVar Variation Id: 1197890
ClinVar RCV Id: RCV001561868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055935.4:p.Thr3155Ser
CA1714662
NM_015120.4:c.9463A>T
CA347275198
NM_015120.4:c.9464C>G