Canonical Allele Identifier: PA658675517
Gene: GCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 462901
ClinVar RCV Id: RCV000540411 RCV001683562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004474.2:p.Asn73Ser
CA8186795
NM_004483.5:c.218A>G