Canonical Allele Identifier: PA645383821
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237188
ClinVar RCV Id: RCV000230242 RCV000487138 RCV000570386 RCV003998729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys1117Phe
CA070699
NM_000179.3:c.3350G>T