Canonical Allele Identifier: PA2826636698
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140848
ClinVar RCV Id: RCV000129055 RCV000205831 RCV000212670 RCV003398753 RCV003997476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu624Phe
CA010886
NM_001281494.2:c.1870C>T