Canonical Allele Identifier: PA2573166467
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1435407
ClinVar RCV Id: RCV002001826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp461Glu
CA389050740
NM_000257.4:c.1383C>A
CA389050741
NM_000257.4:c.1383C>G