Canonical Allele Identifier: PA2826635496
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234553
ClinVar RCV Id: RCV000216304 RCV000567024 RCV001071803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser346Ile
CA10577270
NM_001281494.2:c.1037G>T