Canonical Allele Identifier: PA2826635577
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_001268423.1:p.Ser364Tyr
CA346750659
NM_001281494.2:c.1091C>A