Canonical Allele Identifier: PA132059
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43052
ClinVar RCV Id: RCV000035946 RCV000628865 RCV001185539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1674Met
CA015575
NM_000257.4:c.5020G>A