Canonical Allele Identifier: PA237387
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 191727
ClinVar RCV Id: RCV000172043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1569Asn
CA015240
NM_000257.4:c.4707G>T
CA043659
NM_000257.4:c.4707G>C