Canonical Allele Identifier: PA2499290407
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1030853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Gly304Arg
CA361672735
NM_024577.4:c.910G>C
CA361672737
NM_024577.4:c.910G>A