Canonical Allele Identifier: PA2573192707
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 423124
ClinVar RCV Id: RCV000483635 RCV000547773 RCV001020696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu899_Met900insIle
CA16617704
NM_001281494.2:c.2697_2699dup