Canonical Allele Identifier: PA658803117
Gene: HCCS HGNC NCBI

Linked Data

ClinVar Variation Id: 545079
ClinVar RCV Id: RCV000656298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116080.1:p.Pro54Leu
CA412054275
NM_001122608.3:c.161C>T