Canonical Allele Identifier: PA2826506904
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 6821
ClinVar RCV Id: RCV000007223 RCV000149834 RCV000208379 RCV000213000 RCV000624656 RCV000853278 RCV001813181 RCV002221469 RCV003330311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser2Gly
CA118524
NM_001269039.3:c.4A>G