Canonical Allele Identifier: PA2827651896
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 203759
ClinVar RCV Id: RCV000185950 RCV002513956 RCV004020253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Glu201Gln
CA312603
NM_001352514.2:c.601G>C