ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA658675517
Gene: GCSH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
462901
ClinVar RCV Id:
RCV000540411
RCV001683562
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004474.2:p.Asn73Ser
CA8186795
NM_004483.5:c.218A>G