Canonical Allele Identifier: PA645416938
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407168
ClinVar RCV Id: RCV000469353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1289Gly
CA16614083
NM_000257.4:c.3865C>G