Canonical Allele Identifier: PA916011380
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89357
ClinVar RCV Id: RCV000074823 RCV000162445 RCV000254700 RCV000524159 RCV000709742 RCV000780464 RCV001356266 RCV001564011 RCV003466947 RCV003997086 RCV003162475 RCV003492400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg946Cys
CA012063
NM_001281492.2:c.2836C>T