Canonical Allele Identifier: PA2826627006
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 224581
ClinVar RCV Id: RCV000210157 RCV000215593 RCV001044010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala607Val
CA357802
NM_001281492.2:c.1820C>T