Canonical Allele Identifier: PA2580269761
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2451078
ClinVar RCV Id: RCV003182096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Thr361Ser
CA360268022
NM_002439.5:c.1081A>T
CA360268027
NM_002439.5:c.1082C>G