Canonical Allele Identifier: PA287312
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127586
ClinVar RCV Id: RCV000115414 RCV000122964 RCV000212629 RCV000524173 RCV000656887 RCV001355172 RCV003997249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn112Ser
CA012677
NM_000179.3:c.335A>G