Canonical Allele Identifier: PA196850
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187147
ClinVar RCV Id: RCV000166842 RCV001041140 RCV001797654 RCV001552358 RCV003995537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly723Ala
CA009788
NM_000179.3:c.2168G>C