Canonical Allele Identifier: PA2741935626
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3011897
ClinVar RCV Id: RCV003872960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Phe34Leu
CA5689554
NM_007373.4:c.102T>G
CA378381301
NM_007373.4:c.100T>C
CA378381341
NM_007373.4:c.102T>A