Allele Registry

Canonical Allele Identifier: PA645380717

Gene: MSH6 HGNC NCBI

ClinVar Allele:

405883

616741

ClinVar RCV:

RCV000482393

RCV000580006

RCV000705166

RCV000777254

ClinVar Variation:

418324

631128

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln572His	CA068066 NM_000179.3:c.1716G>T CA46709475 NM_000179.3:c.1716G>C