Canonical Allele Identifier: PA2826625099
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 921148
ClinVar RCV Id: RCV001180403 RCV003759010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn161Lys
CA346740641
NM_001281492.2:c.483C>A
CA346740643
NM_001281492.2:c.483C>G