Canonical Allele Identifier: PA916067004
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_115637.3:p.Glu77Lys
CA10074308
NM_032261.5:c.229G>A