Canonical Allele Identifier: PA2826507172
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373090
ClinVar RCV Id: RCV000413825 RCV001584108 RCV002272224 RCV003922677 RCV003539878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Met173Val
CA16042684
NM_001269039.3:c.517A>G