Canonical Allele Identifier: PA092688
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9891
ClinVar RCV Id: RCV000010569 RCV000085274
ClinVar Variation Id: 940378
ClinVar RCV Id: RCV001209952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Gly109Arg
CA226679
NM_000330.3:c.325G>C
CA412372642
NM_000330.3:c.325G>A