Canonical Allele Identifier: PA346506
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 180432
ClinVar RCV Id: RCV000157350 RCV000464574 RCV000225729 RCV000769466
ClinVar Variation Id: 859306
ClinVar RCV Id: RCV001065383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly178Arg
CA015959
NM_000257.4:c.532G>A
CA389052603
NM_000257.4:c.532G>C