Canonical Allele Identifier: CA2391131815
Gene: CRYAA HGNC NCBI

Linked Data

dbSNP Id: rs1985814700
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43172808C>T , CM000683.2:g.43172808C>T GRCh38
NG_009823.1:g.8778C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000394.3:c.*528C>T NP_000385.1:n.*528C>T
NM_001363766.1:c.*528C>T NP_001350695.1:n.*528C>T
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