Canonical Allele Identifier: PA337668
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216325
ClinVar RCV Id: RCV000198127 RCV000480324 RCV000564851 RCV000663156 RCV003317146 RCV003997005 RCV004530189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly32Cys
CA073625
NM_000179.3:c.94G>T