Canonical Allele Identifier: PA294361
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142305
ClinVar RCV Id: RCV000131354 RCV000167904 RCV000212632 RCV000411184 RCV000708856 RCV001193124 RCV001355774 RCV001535792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp217Gly
CA016133
NM_000179.3:c.650A>G