Canonical Allele Identifier: PA645381686
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234747
ClinVar RCV Id: RCV000223534 RCV000532996 RCV000564357 RCV000758666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg732Gln
CA068599
NM_000179.3:c.2195G>A