Canonical Allele Identifier: PA092626
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98966
ClinVar RCV Id: RCV000085307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Glu146Asp
CA226742
NM_000330.3:c.438G>C
CA412371736
NM_000330.3:c.438G>T