Canonical Allele Identifier: PA2827168319
Gene: GSS HGNC NCBI

Linked Data

ClinVar Variation Id: 1163160
ClinVar RCV Id: RCV001507983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309423.1:p.Pro272Leu
CA408702245
NM_001322494.1:c.815C>T