Canonical Allele Identifier: PA355596
Gene: ALMS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 221028
ClinVar RCV Id: RCV000224685 RCV000434829 RCV000445553 RCV001079318 RCV002408898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055935.4:p.Thr3544Ser
CA349169
NM_015120.4:c.10631C>G
CA347284290
NM_015120.4:c.10630A>T