Canonical Allele Identifier: PA270946
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 157532
ClinVar RCV Id: RCV000144878 RCV000403900 RCV000465654 RCV000488069 RCV001094974 RCV002453463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Met1184Val
CA270944
NM_024577.4:c.3550A>G