Canonical Allele Identifier: PA658804528
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 524949
ClinVar RCV Id: RCV000628859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1595Asn
CA389037643
NM_000257.4:c.4783G>A