Canonical Allele Identifier: PA2741900430
Gene: SPTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2920891
ClinVar RCV Id: RCV003736438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003117.2:p.Glu44Gly
CA343026742
NM_003126.2:c.131A>G