Allele Registry

Canonical Allele Identifier: PA181129

Gene: MYH6 HGNC NCBI

ClinVar RCV:

RCV000154662

RCV000172034

RCV000769431

RCV000999591

RCV001083211

RCV001256735

RCV002408687

RCV003318356

ClinVar Variation:

177985

HGVS (amino-acid)	Matching Registered Transcripts
NP_002462.2:p.Gln277His	CA181127 NM_002471.4:c.831G>T CA389028339 NM_002471.4:c.831G>C