Canonical Allele Identifier: PA294390
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142426
ClinVar RCV Id: RCV000131540 RCV000212631 RCV000656888 RCV000662620 RCV001085010 RCV004544299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His164Pro
CA015726
NM_000179.3:c.491A>C