Canonical Allele Identifier: PA2827068024
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178376
ClinVar RCV Id: RCV000155123 RCV000327761 RCV000756212 RCV003965159
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307967.1:p.Ser580Leu
CA182212
NM_001321038.2:c.1739C>T