Canonical Allele Identifier: PA2499263262
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000782
ClinVar RCV Id: RCV001296955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Arg106Pro
CA408633675
NM_003098.3:c.317G>C