Canonical Allele Identifier: PA2826632238
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142495
ClinVar RCV Id: RCV000131640 RCV000205918 RCV000212672 RCV000412088 RCV001356309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp641Tyr
CA010974
NM_001281493.2:c.1921G>T