Canonical Allele Identifier: PA916011365
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187384
ClinVar RCV Id: RCV000167108 RCV000213713 RCV000805949 RCV003995558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly942Val
CA011990
NM_001281492.2:c.2825G>T