Canonical Allele Identifier: PA197986
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187570
ClinVar RCV Id: RCV000167309 RCV000535861 RCV003995581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met176Val
CA015793
NM_000179.3:c.526A>G