Canonical Allele Identifier: PA2741900863
Gene: SPTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2690081
ClinVar RCV Id: RCV003491545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003117.2:p.Ala2365Val
CA1181732
NM_003126.2:c.7094C>T
CA2697554613
NM_003126.2:c.7094_7095delinsTG