Canonical Allele Identifier: PA210427
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140780
ClinVar RCV Id: RCV000128926 RCV000168003 RCV000202238 RCV000410809 RCV000656890 RCV000761137 RCV003492580 RCV003467099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val250Ala
CA016410
NM_000179.3:c.749T>C