Canonical Allele Identifier: PA2826630092
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485877
ClinVar RCV Id: RCV000562012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly141Val
CA346744502
NM_001281493.2:c.422G>T