Canonical Allele Identifier: PA916011630
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 666858
ClinVar RCV Id: RCV000825371 RCV001211394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala48Pro
CA346741513
NM_001281494.2:c.142G>C