Canonical Allele Identifier: PA182213
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178376
ClinVar RCV Id: RCV000155123 RCV000327761 RCV000756212 RCV003965159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Ser580Leu
CA182212
NM_013296.5:c.1739C>T