Canonical Allele Identifier: PA2830360691
Gene: SHOC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2659431
ClinVar RCV Id: RCV003430205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775792.5:p.Ser196Leu
CA5188946
NM_173521.5:c.587C>T