Canonical Allele Identifier: PA645463875
Gene: SPATC1L HGNC NCBI

Linked Data

ClinVar Variation Id: 403469
ClinVar RCV Id: RCV000455748 RCV001672774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136326.1:p.Glu231Lys
CA10074308
NM_001142854.1:c.691G>A