Canonical Allele Identifier: PA645379516
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 418249
ClinVar RCV Id: RCV000484482 RCV001441245 RCV002525761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Arg302Ser
CA10020590
NM_000411.8:c.906G>C
CA409912051
NM_000411.8:c.906G>T