Canonical Allele Identifier: PA296636
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181236
ClinVar RCV Id: RCV000158623 RCV000780520 RCV001233105 RCV001797640 RCV002484975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1295Lys
CA014200
NM_000257.4:c.3883G>A