Canonical Allele Identifier: PA916011655
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134851
ClinVar RCV Id: RCV000121578 RCV000130273 RCV000409146 RCV000588001 RCV000515340 RCV001083152 RCV001356010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly53Ser
CA007937
NM_001281494.2:c.157G>A