Canonical Allele Identifier: PA658802214
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525592
ClinVar RCV Id: RCV000629678 RCV000774601 RCV004002769
ClinVar Variation Id: 839817
ClinVar RCV Id: RCV001041663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr727Ser
CA068566
NM_000179.3:c.2180C>G
CA346751208
NM_000179.3:c.2179A>T