Canonical Allele Identifier: PA645381515
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428334
ClinVar RCV Id: RCV000491970 RCV003493602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe706Cys
CA346750971
NM_000179.3:c.2117T>G