Canonical Allele Identifier: PA916011684
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485878
ClinVar RCV Id: RCV000566365 RCV002469207 RCV001229506 RCV004001123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp56Glu
CA067120
NM_001281494.2:c.168C>G
CA346741706
NM_001281494.2:c.168C>A