Canonical Allele Identifier: PA097955
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14125
ClinVar RCV Id: RCV000015185 RCV000158569 RCV000469895 RCV000035817 RCV000762923 RCV001181317 RCV000617405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp906Gly
CA012936
NM_000257.4:c.2717A>G