Canonical Allele Identifier: PA916011480
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220784
ClinVar RCV Id: RCV000206715 RCV000508319 RCV000663075 RCV000985259 RCV003468963 RCV004528997 RCV000571369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp982Asn
CA070677
NM_001281492.2:c.2944G>A