Canonical Allele Identifier: PA916011389
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89358
ClinVar RCV Id: RCV000074824 RCV000115409 RCV000121583 RCV000656898 RCV001358430 RCV001085899 RCV001093655 RCV002288561 RCV004528272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro952Leu
CA012135
NM_001281492.2:c.2855C>T