Canonical Allele Identifier: PA645385125
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234450
ClinVar RCV Id: RCV000216522 RCV000567812 RCV000630217 RCV001201279 RCV003998616 RCV003463610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn1327His
CA072425
NM_000179.3:c.3979A>C