Canonical Allele Identifier: PA132104
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43082
ClinVar RCV Id: RCV000035977 RCV000242151 RCV000263236 RCV000325552 RCV000331432 RCV000369831 RCV000758073 RCV001094151 RCV001311852 RCV003320088 RCV004541083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1902Gln
CA016398
NM_000257.4:c.5704G>C