Canonical Allele Identifier: PA2826630513
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491876
ClinVar RCV Id: RCV000584667 RCV001067724 RCV003465311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys241Arg
CA346747119
NM_001281493.2:c.722A>G