Canonical Allele Identifier: PA2826629627
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 336441
ClinVar RCV Id: RCV000292993 RCV000524218 RCV001189629 RCV002480193 RCV002509369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr31Ala
CA10615752
NM_001281493.2:c.91A>G