Canonical Allele Identifier: PA108742
Gene: SPTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2433756
ClinVar RCV Id: RCV003132655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003117.2:p.Arg45Thr
CA343026736
NM_003126.2:c.134G>C