Canonical Allele Identifier: PA092439
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98958
ClinVar RCV Id: RCV000085299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Arg141Gly
CA226726
NM_000330.3:c.421C>G