Canonical Allele Identifier: PA185991
Gene: CERS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 183023
ClinVar RCV Id: RCV000161146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067090.1:p.His183Gln
CA185990
NM_021267.5:c.549C>G
CA404866886
NM_021267.5:c.549C>A