Canonical Allele Identifier: PA2573082483
Gene: SNTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310685
ClinVar RCV Id: RCV001767799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003089.1:p.Lys109Asn
CA408633651
NM_003098.3:c.327G>T
CA408633652
NM_003098.3:c.327G>C