Canonical Allele Identifier: PA2827251305
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3011897
ClinVar RCV Id: RCV003872960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311266.1:p.Phe34Leu
CA5689554
NM_001324337.2:c.102T>G
CA378381301
NM_001324337.2:c.100T>C
CA378381341
NM_001324337.2:c.102T>A