Canonical Allele Identifier: PA658804411
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 524975
ClinVar RCV Id: RCV000628910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu387Phe
CA389051219
NM_000257.4:c.1159C>T