Canonical Allele Identifier: PA2825087588
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 919753
ClinVar RCV Id: RCV001178071
ClinVar Variation Id: 3230488
ClinVar RCV Id: RCV004520639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu337Phe
CA346741258
NM_000179.3:c.1011G>C
CA346741261
NM_000179.3:c.1011G>T