Canonical Allele Identifier: PA108728
Gene: SPTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12849
ClinVar RCV Id: RCV000013702 RCV000013703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003117.2:p.Arg45Ser
CA122752
NM_003126.2:c.135G>T
CA343026734
NM_003126.2:c.135G>C