Canonical Allele Identifier: PA916010025
Gene: SPRR2A HGNC NCBI

Linked Data

ClinVar Variation Id: 782388
ClinVar RCV Id: RCV000963772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005979.1:p.Thr20Lys
CA1113715
NM_005988.3:c.59C>A