ClinGen Allele Registry
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Canonical Allele Identifier:
PA645414194
Gene: SH3TC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
265353
ClinVar RCV:
RCV000558978
RCV000723677
RCV000789696
RCV001157494
RCV001157495
RCV001706410
RCV002379107
RCV003319193
ClinVar Variation:
281116
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_078853.2:p.Ser433Leu
CA3499208
NM_024577.4:c.1298C>T