Canonical Allele Identifier: PA916068780
Gene: SNURF HGNC NCBI

Linked Data

ClinVar Variation Id: 315438
ClinVar RCV Id: RCV000295889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073715.1:p.Arg7Cys
CA7431173
NM_022804.3:c.19C>T