ClinGen Allele Registry
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Canonical Allele Identifier:
PA098388
Gene: MYH7
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000015154
RCV000158521
RCV000158522
RCV000243586
RCV000461730
RCV000472342
RCV000621362
RCV001170499
RCV001170500
RCV002490371
RCV004534738
ClinVar Variation:
14098
42890
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000248.2:p.Gly741Arg
CA012004
NM_000257.4:c.2221G>A
CA012013
NM_000257.4:c.2221G>C