Canonical Allele Identifier: PA658804414
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 519201
ClinVar RCV Id: RCV000621111 RCV003586209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu395Arg
CA389051166
NM_000257.4:c.1184T>G