Canonical Allele Identifier: PA645432817
Gene: MYH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 263719
ClinVar RCV Id: RCV000247796 RCV002487142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002462.2:p.Phe1898Val
CA10587756
NM_002471.4:c.5692T>G