Canonical Allele Identifier: PA2826627987
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234533
ClinVar RCV Id: RCV000214691 RCV000461768 RCV000573070 RCV000657064 RCV003153515 RCV003998622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile837Val
CA10577283
NM_001281492.2:c.2509A>G