Canonical Allele Identifier: PA168549
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142508
ClinVar RCV Id: RCV000131657 RCV000214572 RCV000410793 RCV000472070 RCV000656889 RCV003467180 RCV003998114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser238Tyr
CA016318
NM_000179.3:c.713C>A