Canonical Allele Identifier: PA1139724576
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 948490
ClinVar RCV Id: RCV001219754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Gly384Ser
CA360268299
NM_002439.5:c.1150G>A