Canonical Allele Identifier: PA916012238
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824191
ClinVar RCV Id: RCV001021103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gln956His
CA346761135
NM_001281494.2:c.2868A>T
CA346761137
NM_001281494.2:c.2868A>C