Canonical Allele Identifier: PA2741935607
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2749309
ClinVar RCV Id: RCV003540262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Pro16Arg
CA5689548
NM_007373.4:c.47C>G