Canonical Allele Identifier: PA2826626700
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 627999
ClinVar RCV Id: RCV000772273 RCV001346051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser536Tyr
CA346750659
NM_001281492.2:c.1607C>A