Canonical Allele Identifier: PA645378776
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410485
ClinVar RCV Id: RCV000507572 RCV002230119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser242Thr
CA16610926
NM_000179.3:c.725G>C