Canonical Allele Identifier: PA2741935652
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2957705
ClinVar RCV Id: RCV003811368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Arg190Lys
CA5689597
NM_007373.4:c.569G>A