Canonical Allele Identifier: PA1139724355
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 944450
ClinVar RCV Id: RCV001214850 RCV002402639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asp351Asn
CA3327788
NM_002439.5:c.1051G>A