Canonical Allele Identifier: PA916035381
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_001339443.1:p.Arg449Ser
CA10020590
NM_001352514.2:c.1347G>C
CA409912051
NM_001352514.2:c.1347G>T