Canonical Allele Identifier: PA2573221894
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512483
ClinVar RCV Id: RCV002045663 RCV002398107 RCV003464389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Ala353Thr
CA360267923
NM_002439.5:c.1057G>A