Canonical Allele Identifier: PA2573221902
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1412247
ClinVar RCV Id: RCV001919042 RCV002407065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asn355Lys
CA360267953
NM_002439.5:c.1065T>A
CA360267956
NM_002439.5:c.1065T>G