Canonical Allele Identifier: PA916011970
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455266
ClinVar RCV Id: RCV000543217 RCV000572853 RCV000588973 RCV003470704 RCV004003694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro867Ala
CA46717040
NM_001281494.2:c.2599C>G