Canonical Allele Identifier: PA2826636004
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 801698
ClinVar RCV Id: RCV000986721 RCV001351789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His464Gln
CA068773
NM_001281494.2:c.1392T>G
CA346753012
NM_001281494.2:c.1392T>A