Canonical Allele Identifier: PA180115
Gene: HGSNAT HGNC NCBI

Linked Data

ClinVar Variation Id: 167177
ClinVar RCV Id: RCV000153362 RCV000670920 RCV001243388 RCV001815238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689632.2:p.Pro237Gln
CA180114
NM_152419.3:c.710C>A