Canonical Allele Identifier: PA2826632220
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453185
ClinVar RCV Id: RCV003182640 RCV003759794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp636Glu
CA346755638
NM_001281493.2:c.1908C>A
CA346755640
NM_001281493.2:c.1908C>G