Canonical Allele Identifier: PA2826625665
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 336442
ClinVar RCV Id: RCV000300787 RCV000688085 RCV000564277 RCV001571224 RCV003995876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu293Ile
CA10615505
NM_001281492.2:c.877C>A