Canonical Allele Identifier: PA2580462790
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1937489
ClinVar RCV Id: RCV002653292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078853.2:p.Met999Val
CA361665162
NM_024577.4:c.2995A>G