Canonical Allele Identifier: PA645461589
Gene: LIPH HGNC NCBI

Linked Data

ClinVar Variation Id: 225403
ClinVar RCV Id: RCV000023645 RCV000490454 RCV000826145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_640341.1:p.Cys246Ser
CA2740507
NM_139248.3:c.736T>A
CA355688734
NM_139248.3:c.737G>C