Canonical Allele Identifier: PA092963
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98941
ClinVar RCV Id: RCV000085281
ClinVar Variation Id: 98942
ClinVar RCV Id: RCV000085282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Trp112Cys
CA226694
NM_000330.3:c.336G>C
CA226696
NM_000330.3:c.336G>T