Canonical Allele Identifier: PA092981
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9886
ClinVar RCV Id: RCV000010564 RCV000085262 RCV001074398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Trp96Arg
CA226653
NM_000330.3:c.286T>C
CA412372774
NM_000330.3:c.286T>A