Canonical Allele Identifier: PA645417654
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407198
ClinVar RCV Id: RCV000468219 RCV001185798 RCV002339146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1662Leu
CA16614388
NM_000257.4:c.4985G>T