Canonical Allele Identifier: PA645378414
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418320
ClinVar RCV Id: RCV000482046 RCV000553070 RCV001183214 RCV004002246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His130Arg
CA16617626
NM_000179.3:c.389A>G