Canonical Allele Identifier: PA2826632135
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418328
ClinVar RCV Id: RCV000480774 RCV000774604 RCV001071302 RCV003387852 RCV003470525 RCV004002247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.His616Arg
CA069591
NM_001281493.2:c.1847A>G