Canonical Allele Identifier: PA645417527
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407190
ClinVar RCV Id: RCV000468415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1615Asn
CA16614393
NM_000257.4:c.4845G>T
CA389037525
NM_000257.4:c.4845G>C