Canonical Allele Identifier: PA1139673773
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 920877
ClinVar RCV Id: RCV001179928 RCV001875960 RCV002320400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1042Arg
CA257817945
NM_000257.4:c.3125A>G