Canonical Allele Identifier: PA2826632799
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182645
ClinVar RCV Id: RCV000232219 RCV000562784 RCV000587626 RCV003488409 RCV003998502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met772Val
CA012035
NM_001281493.2:c.2314A>G