Canonical Allele Identifier: PA207079
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 211558
ClinVar RCV Id: RCV000193528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1629Pro
CA207077
NM_000257.4:c.4886T>C