Canonical Allele Identifier: PA645383970
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419014
ClinVar RCV Id: RCV000478492 RCV000561997 RCV000758613 RCV000820952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1148Ser
CA070946
NM_000179.3:c.3442G>A